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The exothermic (heat producing) reaction between potassium permanganate (KMnO 4), a strong oxidizing agent, and glycerol (C 3 H 5 (OH) 3), a readily oxidised organic substance, is an example of an experiment sometimes referred to as a "chemical volcano". [7] [8]
5 c 6 h 5 ch 3 + 6 kmno 4 + 9 h 2 so 4 → 5 c 6 h 5 cooh + 14 h 2 o + 3 k 2 so 4 + 6 mnso 4 Glycols and polyols are highly reactive toward KMnO 4 . For example, addition of potassium permanganate to an aqueous solution of sugar and sodium hydroxide produces the chemical chameleon reaction, which involves dramatic color changes associated with ...
The industrial route entails treatment of MnO 2 with air and potassium hydroxide: [1] 2 MnO 2 + 4 KOH + O 2 → 2 K 2 MnO 4 + 2 H 2 O. The transformation gives a green-colored melt. Alternatively, instead of using air, potassium nitrate can be used as the oxidizer: 2 KOH + KNO 3 + MnO 2 → K 2 MnO 4 + H 2 O + KNO 2
When used to oxidize organic compounds, the exact chemical reaction depends on the organic reactant present. For example, trichloroethane (C 2 H 3 Cl 3) is oxidised by permanganate ions to form carbon dioxide (CO 2), manganese dioxide (MnO 2), hydrogen ions (H +), and chloride ions (Cl −). [6] 8 MnO − 4 + 3 C 2 H 3 Cl 3 → 6 CO 2 + 8 MnO 2 ...
[1] Ammonium permanganate decomposes explosively to manganese dioxide, nitrogen, and water: [2] 2 NH 4 MnO 4 → 2 MnO 2 + N 2 + 4 H 2 O. Ammonium permanganate decomposes slowly in storage even at normal temperatures. A sample stored for 3 months was only 96% pure, after 6 months it assumed color of iodine and had strong smell of nitrogen oxides.
Permanganic acid has also been prepared through the reaction of hydrofluorosilicic acid with potassium permanganate, [4] through electrolysis, and through hydrolysis of manganese heptoxide, though the last route often results in explosions. [5] Crystalline permanganic acid has been prepared at low temperatures as the dihydrate, HMnO 4 ·2H 2 O. [3]
Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.
2 KNO 3 + 5 Mg → K 2 O + N 2 + 5 MgO. The composition is 62.4% KNO 3 : 37.6% Mg by weight for the reactants of the above stoichiometrically balanced equation. Below is the same reaction but involving barium nitrate. Ba(NO 3) 2 + 5 Mg → BaO + N 2 + 5 MgO. Mixtures designed to make reports are substantially different from mixtures designed ...